VAERS 2021 Database www.vaers.hhs.gov

Main Page | All 2021 Deaths | Videos
VAERS Updated: 11/12/2021
** VAERS DATABASE Last updated: November 12, 2021**
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Manufacturers

Total Manufacturer
46,870MODERNA
532GLAXOSMITHKLINE BIOLOGICALS
353PFIZER\BIONTECH
231MERCK & CO. INC.
221UNKNOWN MANUFACTURER
62SEQIRUS, INC.
25DYNAVAX TECHNOLOGIES CORPORATION
13EMERGENT BIOSOLUTIONS
12SANOFI PASTEUR
9NOVARTIS VACCINES AND DIAGNOSTICS
5PFIZER\WYETH
5PAXVAX
2TEVA PHARMACEUTICALS
2PROTEIN SCIENCES CORPORATION
1BERNA BIOTECH, LTD.
1INTERCELL AG
1CSL LIMITED

COVID19 Lot Number

VAX LOT Total
2S9CL1,906
1,575
289
IMM209286
252
236
229
s029456178
171
UT7065MA166
155
149
145
S034636133
107
U62828AA103
100
98
P10025327596
U6737AA85
UJ446AA79
78
78
59
57
4BH3254
4F47253
52
27656352
50
PP9L548
49TM346
42
40
38
MENVEO38
4F47237
R1B252M36
34
C5763AA30
93362229
25
300057A24
UNK24
22
CW311621
18
17
15
UH894AB15
3Y7NL12
R1B743M12
EJ168611
el128410
10
10
10
9
ARBA141A9
UNK9
8
UNK8
8
1F4EB8
Unknown7
7
No batch number6
5
5
UJ090AA5
5
5
4
4
4
UNK4
JEV18K95E4
UNK3
A115A3
Z127A3
3
3333324181073
2
2
2
TAR352
1
1
1
1
1
A739081
1
1
1
1
1
037K20A68,542
EL128447,700
133

Incidents per State

State Total
15,185
CA14,096
NY7,507
TX7,196
FL6,939
IN5,527
PA4,560
IL4,179
OH4,054
AZ3,856
MI3,771
NJ3,411
MA3,278
VA3,208
NC3,114
WA3,034
GA2,864
MD2,652
MN2,534
CO2,532
WI2,457
MO2,029
OR1,943
TN1,715
CT1,693
KY1,603
OK1,226
AL1,201
KS1,162
IA1,157
SC1,106
NM1,065
UT973
AR951
LA945
NE829
NV797
ME795
MT789
NH756
ID674
AK661
WV661
PR650
MS585
HI536
RI510
VT441
SD361
ND356
DE350
DC239
WY209
GU32
AS16
VI13
MP9
MH3
FM2
QM1
XB1

ID: 1000156
Sex: F
Age:
State: IN

Vax Date: 12/30/2020
Onset Date: 12/31/2020
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210109; Test Name: covid; Test Result: Positive ; Test Date: 20210107; Test Name: Nasal PCR Test; Test Result: Positive

Allergies:

Symptoms: I tested positive for covid on 09Jan2021; I tested positive for covid on 09Jan2021; Fatigue, sore arm up to 48 hours post injection. Started feeling feverish with chills on 03Jan2021. I tested positive for covid on 09Jan2021; Fatigue, sore arm up to 48 hours post injection. Started feeling feverish with chills on 03Jan2021. I tested positive for covid on 09Jan2021; Fatigue, sore arm up to 48 hours post injection. Started feeling feverish with chills on 03Jan2021. I tested positive for covid on 09Jan2021; Fatigue, sore arm up to 48 hours post injection. Started feeling feverish with chills on 03Jan2021. I tested positive for covid on 09Jan2021; This is a spontaneous report from a contactable nurse. A 47-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, batch/lot number EK5730), intramuscular in Left arm on 30Dec2020 17:00 at single dose for covid-19 immunisation. Medical history included asthma (as a child). Concomitant medication included loratadine (CLARITIN [LORATADINE]), cyanocobalamin (B12 [CYANOCOBALAMIN]), fluticasone propionate (FLONASE [FLUTICASONE PROPIONATE]). The patient previously took morphine and experienced Known allergies. The patient experienced fatigue, sore arm up to 48 hours post injection. Started feeling feverish with chills on 03Jan2021. I tested positive for covid on 09Jan2021. The patient received just fluids, vit c,zinc, and vitd as treatment. No covid prior vaccination. Covid tested post vaccination. The patient underwent lab tests and procedures which included sars-cov-2 test: positive on 09Jan2021, sars-cov-2 test: positive on 07Jan2021. The outcome of the event Feverish and Chills was resolved on Jan2021, Vaccination site pain and Fatigue was resolved on an unspecified date, while the outcome of the other events was unknown.

Other Meds: CLARITIN [LORATADINE]; B12 [CYANOCOBALAMIN]; FLONASE [FLUTICASONE PROPIONATE]

Current Illness:

ID: 1000157
Sex: M
Age:
State: CT

Vax Date: 01/15/2021
Onset Date: 01/15/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210115; Test Name: Heart rate; Result Unstructured Data: Test Result:High

Allergies:

Symptoms: About 5-7 minutes after vaccination I felt very weak and dizzy; About 5-7 minutes after vaccination I felt very weak and dizzy; Saw stars, and very high heart rate; Saw stars, and very high heart rate; This is a spontaneous report from a contactable other hcp (patient). A 21-year-old male patient received first dose of bnt162b2 (BNT162B2) , via an unspecified route of administration on 15Jan2021 10:00 at single dose on left arm for covid-19 immunisation. Medical history included ongoing penicillin allergy. There were no concomitant medications. The patient stated that, "About 5-7 minutes after vaccination I felt very weak and dizzy. Saw stars, and very high heart rate" on 15Jan2021 10:00. No other vaccine in four weeks, no other medications in two weeks. No COVID prior vaccination, no COVID tested post vaccination. No treatment was received for the events. The outcome of the events was resolved in Jan2021. Information about batch/lot number has been requested.

Other Meds:

Current Illness: Penicillin allergy

ID: 1000158
Sex: F
Age:
State: MS

Vax Date: 01/09/2021
Onset Date: 01/09/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210111; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptoms: Fever; chills; body aches; muscle aches; headaches; This is a spontaneous report from a contactable Health Professional, the patient. A 34-year-old non-pregnant female received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via intramuscular route in the right arm on 09Jan2021 at 11:45 as a single dose for COVID-19 immunization. The patient's medical history was not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not have any allergies to medications, food, or other products. Historical Vaccine data included the first dose of BNT162B2 on an unknown date for COVID-19 immunization. The patient's concomitant medications were not reported. The patient did not receive any other vaccine within 4 weeks prior to the vaccine. On 09Jan2021 at 20:00, the patient experienced fever, chills, body aches, muscle aches, and headaches. The patient did not receive treatment for the events. Since the vaccination, the patient had tested for COVID-19 via Nasal Swab on 11Jan2021 with a Negative result. The clinical outcome of the events, fever, chills, body aches, muscle aches, and headaches was recovered in Jan2021. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1000159
Sex: M
Age:
State: GA

Vax Date: 01/14/2021
Onset Date: 01/19/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: lost partial vision in my left eye for 10 minutes; tunnel vision; This is a spontaneous report from a contactable consumer reported for himself. A 65-year-old male patient received first dose of BNT162B2(PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3302), via an unspecified route of administration on 14Jan2021 16:00 at single dose, left arm for covid-19 immunization. Medical history reported as none. The patient's concomitant medications were not reported. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Allergies to medications, food, or other products reported as No. The patient experienced "lost partial vision in my left eye for 10 minutes" and tunnel vision on 19Jan2021 18:00 with outcome of recovered. On January 19th at 6 pm, the patient had lost partial vision in his left eye for 10 minutes. He had tunnel vision. The patient went to his eye doctor yesterday and his vision was fine with not noticeable issues. No treatment received for the adverse event. Events reported as non-serious. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19.

Other Meds:

Current Illness:

ID: 1000160
Sex: M
Age:
State:

Vax Date: 01/18/2021
Onset Date: 01/01/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 202101; Test Name: fever; Result Unstructured Data: Test Result:100.9 Fahrenheit; Comments: high; Test Date: 202101; Test Name: fever; Result Unstructured Data: Test Result:normal Fahrenheit

Allergies:

Symptoms: fever (high 100.9 fahrenheit); chills; nausea; This is a spontaneous report from a non-contactable consumer via a sales representative. A 51-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiry date unknown) via unspecified route of administration on 18Jan2021 at single dose for Covid-19 immunization. The patient medical history was not reported. The patient's concomitant medications was none. The patient's historical vaccine included first dose of BNT162B2 on 28Dec2020 for Covid-19 immunization. The patient experienced fever (high 100.9 fahrenheit), chills, and nausea following second dose approximately 12 hours after dose (Jan2021) and falling to normal at approximately 36 hours (Jan2021). The patient received Tylenol 500 mg twice taken for fever every eight hours. The outcome of the event fever (high 100.9 fahrenheit), chills, and nausea was recovered on Jan2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1000161
Sex: M
Age:
State: CA

Vax Date: 12/25/2020
Onset Date: 12/27/2020
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Patient did not receive the 2nd dose as scheduled; Sick; Hearing loss (left ear); This is a spontaneous report from a Pfizer-sponsored program from a contactable consumer reporting for himself. A 63 (unit unspecified) male patient received the 1st dose of bnt162b2 (BNT162B2, Manufacturer Pfizer-BioNTech), via an unspecified route of administration, on 25Dec2020, at single dose, for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient experienced hearing loss (left ear) on 27Dec2020 with outcome of recovering. He only had 60% hearing. Therapeutic measures were taken as a result of the event and included treatment with unspecified medication. Now hearing was 90% back. Furthermore, the patient did not receive the 2nd dose on 16Jan2021 as scheduled as he was sick. The reporter stated that he didn't know if hearing loss (left ear) had to do with the vaccine. He asked the doctor, he didn't know either, he said it could be stress or virus. The information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1000162
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: extreme fatigue; chills; This is a spontaneous report from a non-contactable other HCP communicated to a Pfizer colleague. A patient (demographics unknown), received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection) on an unspecified date at single dose via an unspecified route of administration for COVID-19 immunization. Relevant medical history and concomitant medications were not reported. On an unspecified date after the 1st dose of vaccine, patient experienced extreme fatigue and chills. She was knocked out for like 4 hours (as reported). At the time of the reporting event outcome was unknown. No follow-up attempts are possible. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1000163
Sex: F
Age:
State: GA

Vax Date: 01/20/2021
Onset Date: 01/21/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Severe headache; This is a spontaneous report from a non-contactable consumer. A 47-year-old female patient (pregnant no) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 20Jan2021 for second dose at single dose at right arm for COVID-19 immunization. The first dose was on 30Dec2020 on left arm for COVID-19 immunization, at age of 47-year-old. Medical history included cancer (former cancer patient). Allergies to medications, food, or other products was unknown. The patient was not pregnant at the time of vaccination. It was unknown if the patient receive any other vaccines within 4 weeks prior to the COVID vaccine. Concomitant medication included levothyroxine sodium (SYNTHROID), estradiol (ESTROGEN). The patient experienced severe headache lasting all day and currently since this morning when she woke up on 21Jan2021 06:00. Seriousness criteria was not results in death, life threatening, caused/prolonged hospitalization, disabling/incapacitating, congenital anomaly/birth defect. Prior to vaccination and since the vaccination, the patient was not diagnosed with COVID-19. There was no treatment received for the adverse event. The outcome of the event was recovering. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: SYNTHROID; ESTROGEN

Current Illness:

ID: 1000164
Sex: M
Age:
State: NY

Vax Date: 01/19/2021
Onset Date: 01/01/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Body ache; Coughing; This is a spontaneous report from a Pfizer-sponsored Program. A contactable other healthcare professional reported that a male patient (reporter's husband) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) Solution for injection (lot number and expiry date unknown), via an unspecified route of administration on 19Jan2021 at single dose for COVID-19 immunization. The patient's medical history included diabetes mellitus from an unknown date and unknown if ongoing. The patient tested positive in COVID-19 prior to getting the first dose. Concomitant medications were not reported. After taking the vaccine, the patient was having side effects like body ache and coughing on Jan2021. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1000165
Sex: M
Age: 39
State:

Vax Date: 02/03/2021
Onset Date: 02/04/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies: none

Symptoms: chills, muscle pain at site of injection and generally, fatigue, headache, woke from sleep at 2 AM, continued through that day

Other Meds: pantoprazole 40mg

Current Illness: none

ID: 1000166
Sex: M
Age:
State: NY

Vax Date:
Onset Date:
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: headache; This is a spontaneous report from a Pfizer sponsored program via a contactable consumer reported for himself. A male patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiry date unknown) via unspecified route of administration on unspecified date at single dose for Covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced headache on unspecified date. The patient took a Tylenol for his headache a few hours before the shot. The outcome of the event was unknown. Follow-up activities are possible, information on the batch number has been requested.

Other Meds:

Current Illness:

ID: 1000167
Sex: M
Age:
State:

Vax Date: 01/20/2021
Onset Date: 01/21/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: My nose started bleeding this afternoon about an hour ago/start walking it starts bleeding again; This is a spontaneous report from a contactable consumer reported for himself. This male consumer of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 20Jan2021 14:00 at single dose for COVID-19 immunisation. The medical history and concomitant medications were not reported. The consumer reported nose started bleeding in the afternoon about an hour before on 21Jan2021. When the consumer start walking it started bleeding again. The consumer was on clopidogrel bisulfate (PLAVIX). The outcome of the event was unknown. The event was non-serious. Information on the Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1000168
Sex: F
Age:
State: NJ

Vax Date: 12/21/2020
Onset Date: 12/23/2020
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20201223; Test Name: heart rate; Result Unstructured Data: Test Result:Increase; Comments: Increase in heart rate upon standing; Test Date: 20210101; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptoms: Developed palpitations with orthostatic Increase in heart rate upon standing; Developed palpitations with orthostatic Increase in heart rate upon standing; Concern for postural orthostatic tachycardia/POTs; This is a spontaneous report from a contactable Physician (patient). A 53-year-old female patient (not pregnant) received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), Lot number: EL0140, intramuscularly on 21Dec2020 07:30 at single dose in Left arm for COVID-19 immunization in hospital. Medical history was none, no known allergies. Patient didn't have covid prior vaccination. There were no concomitant medications. There were no other vaccines in four weeks and no other medications in two weeks. The patient developed palpitations with orthostatic increase in heart rate upon standing. Concern for postural orthostatic tachycardia/POTs. Adverse events started from 23Dec2020, 07:00 AM and resulted in doctor or other healthcare professional office/clinic visit. No treatment was received for the events. The patient had not recovered from the events. Covid test with nasal swab type post vaccination was performed on 01Jan2021 with negative result.

Other Meds:

Current Illness:

ID: 1000169
Sex: F
Age: 50
State:

Vax Date: 01/21/2021
Onset Date: 01/21/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: None

Allergies: Raw almonds

Symptoms: Pain at the injection site that radiated down the arm and up the neck. Body aches inside and out. Restlessness. All for about 24 hours

Other Meds: Hydrochlorathiazide

Current Illness: None

ID: 1000170
Sex: M
Age:
State: FL

Vax Date: 01/12/2021
Onset Date: 01/18/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: diagnosed with pneumonia; This is a spontaneous report from a contactable consumer via Pfizer Sponsored Program. A 73-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 12Jan2021 at single dose for COVID-19 immunisation at the age of 73-year-old. Lot number was EL1284. There was no medical history nor concomitant medications. The patient experienced pneumonia on 18Jan2021. Pneumonia was diagnosed at check up on 25Jan2021. They were not thinking patient got the pneumonia after the vaccine, they did not know if he had the pneumonia already or not at the time of vaccination. The outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 1000171
Sex: F
Age:
State: MA

Vax Date: 01/13/2021
Onset Date: 01/18/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Rash was reported as worsened.; she has developed a rash all over her face, arm, chest, and belly; The rash is just red, raised, and itchy; The rash is just red, raised, and itchy; This is a spontaneous report from a contactable Nurse (patient). The 61-years-old female patient received first dose of bnt162b2 (BNT162B2, lot number: EL3248, Expiry Date: 01Apr2021), unknown in right deltoid on 13Jan2021 at SINGLE DOSE for covid-19 immunisation. Medical history included Patient History: No. No allergies. There were no concomitant medications. The Caller, an LPN, reporting on the COVID 19 Vaccine and who explains she had it on 13Jan2021. Starting Friday into the weekend and through today she has developed a rash all over her face, arm, chest, and belly on 18Jan2021. The only thing that she can figure is the injection. She was told to call and report this. There has been no treatment, due to the holiday everything is closed. The rash is just red, raised, and itchy and driving her crazy. It is not anything too terrible, just uncomfortable. Rash was reported as worsened. No visit to emergency room or physician office. The outcome of the event condition aggravated was unknown and was not recovered or the rest events. No follow-up attempts possible. No further information expected.

Other Meds:

Current Illness:

ID: 1000172
Sex: F
Age: 55
State: CT

Vax Date: 02/03/2021
Onset Date: 02/03/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: None

Allergies: Hazelnuts

Symptoms: Immediate rapid swelling at injection site (golfball-sized within a minute), fever 101, headache, injection site pain, myalgias

Other Meds: Synthroid, Diltiazem, Lexapro

Current Illness: None

ID: 1000173
Sex: M
Age:
State: SC

Vax Date:
Onset Date:
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Headache; This is a spontaneous report from a contactable Health Professional, the patient. A male patient of an unspecified age received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration on an unknown date as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient experienced headache. The clinical outcome of the event headache was not recovered. No follow-up attempts are possible; information about lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 1000174
Sex: M
Age:
State: NY

Vax Date: 12/01/2020
Onset Date: 01/20/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210120; Test Name: covid; Result Unstructured Data: Test Result:contracted covid virus

Allergies:

Symptoms: dementia; contracted the covid virus; contracted the covid virus; This is a spontaneous report from a Pfizer sponsored program. A contactable consumer (patient's wife) reported that a male patient of an unspecified age received BNT162B2 (Pfizer-BIONTECH Covid-19 Vaccine), with first dose in Dec2020 and with second dose on 19Jan2021, both via an unspecified route of administration at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. It was reported that the patient received BNT162B2 3 weeks ago and got second dose on 19Jan2021, patient had dementia and contracted the COVID virus on 20Jan2021, patient had exposed to COVID 24-48 hours by a healthcare professional in the facility. The outcome of events was unknown. Information on the Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1000175
Sex: F
Age: 38
State: VA

Vax Date: 01/21/2021
Onset Date: 01/29/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: none

Allergies: none

Symptoms: Eight days after injection, I got a hard, red, swollen, itchy bump at injection site. It was a 4 inch square that was warm to the touch.

Other Meds: Vitamin C, Vitamin B, Zinc

Current Illness: none

ID: 1000176
Sex: F
Age:
State: IN

Vax Date: 01/14/2021
Onset Date: 01/14/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210115; Test Name: Body temperature; Result Unstructured Data: Test Result:99.8; Test Date: 20210115; Test Name: Body temperature; Result Unstructured Data: Test Result:103; Test Date: 20210116; Test Name: Body temperature; Result Unstructured Data: Test Result:Fine; Test Date: 20210116; Test Name: Body temperature; Result Unstructured Data: Test Result:97.2

Allergies:

Symptoms: Starred to get blurred vision like a migraine; Fever/temperature was 99.8 then later that day it was 103; Sweat some during sleep, which was pretty normal; No sleep; This is a spontaneous report from a contactable Consumer (patient). An 81-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number: EL1284; Expiry Date: 30Apr2021) on 14Jan2021 at SINGLE DOSE in the right arm for covid-19 immunisation, so she did not get the virus. Medical history included Inflammatory bowel disease. There were no concomitant medications. she was allergic to Sulfa. She had no sleep the first night on 14Jan2021. The next day on 15Jan2021 she had a fever. Her temperature was 99.8 then later that day it was 103. She took an Aspirin. Friday night on 15Jan2021, she slept alright but sweat some, which was pretty normal. Saturday morning on 16Jan2021, her temperature was fine but she starred to get blurred vision like a migraine. She took another Aspirin and it went away. Later that day her temperature was normal at 97.2. She was a pretty active person. After she had the shot around 8 AM-10 AM in the morning, at 12 or 1230 she went out and took down her Christmas lights and she thought she felt good so she was going to trim her plants and she wondered if that had anything to do with her adverse events. Her arm did not hurt or anything. She is wondering if her activity had anything to do with disrupting the medicine? She was using that arm a lot, she probably should not have done it. She will not do it again. The outcome of Starred to get blurred vision like a migraine was recovered on 16Jan2021, of other events were recovered on 15Jan2021.

Other Meds:

Current Illness:

ID: 1000177
Sex: F
Age:
State: AZ

Vax Date: 12/26/2020
Onset Date:
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: sore on in the injection site; This is a spontaneous report from a contactable other healthcare professional (HCP) (patient). A 49-year-old female patient (not pregnant) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration in the right arm on 26Dec2020 08:30 AM at a single dose as COVID vaccine. Medical history included seasonal allergy and high blood pressure. Concomitant medications were not reported. The patient had no other vaccine in four weeks. The patient previously had known allergies to amlodipine. The patient experienced sore on in the injection site on an unspecified date. Treatment was not received for the event. She has no COVID prior to vaccination. She did not have COVID tested post vaccination. The outcome of the event was recovering. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1000178
Sex: F
Age: 40
State:

Vax Date: 01/25/2021
Onset Date: 02/01/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Sore arm 2 days immediately following the shot. New onset erythema Lupper arm at 8days post vaccine. Redness has spread down over 1/3 of lateral portion of L upper arm, with slight tenderness, tender lymph node behind L ear.

Other Meds: none

Current Illness: none

ID: 1000179
Sex: F
Age:
State: SC

Vax Date: 01/15/2021
Onset Date: 01/15/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210117; Test Name: Heart rate; Result Unstructured Data: Test Result:Increased

Allergies:

Symptoms: more tired; Weakness; increased heart rate; Diarrhea; soreness at the injection site; Runny nose; This is a spontaneous report from a contactable Nurse (patient). A 64-year-old female patient received BNT162B2 (Pfizer BioNTech COVID-19 vaccine), intramuscularly on 15Jan2021 at single dose into the left arm for COVID-19 prophylaxis. Medical history included asthma; blood pressure abnormal (she takes blood pressure medication); palpitations at times; having mild chest discomfort, had experienced this before, that she was attributing to her wearing a mask, she wore 2-3 masks; stated that she had Covid once and she did not want it again. Concomitant medications included some blood pressure medication, and salbutamol (ALBUTEROL) inhaler periodically. Caller is a LPN nurse that was calling about the Covid-19 vaccine and reported that she received it Friday 15Jan2021 and just wanted to report some mild side effects. Caller clarified that she was more tired, had weakness, had diarrhea for 2 days, increased heart rate, and a runny nose, soreness at the injection site . She stated that she was not in a lot of distress. More tired started from 17Jan2021 and soreness at the injection site started from 16Jan2021. Weakness started from 17Jan2021: She stated that went home straight from work and went to the couch and slept about 6 hours. She had been up since 0300 and it was almost 1200 now. She stated that her energy level and weakness was pretty good right now. Diarrhea started from 16Jan2021: She said that she had the urgency to go and it was definitely soft and foul like when you had the flu. She stated that she has had it once since this morning. It was semisolid. Increased heart rate started from 17Jan2021: she felt palpitations at times. She said that she did not know if they were related, but stated that they were aggravating yesterday. She stated that she took blood pressure medication. She stated that she used a inhaler albuterol. She was using her inhaler periodically and said that it could be because of the albuterol inhaler. Runny nose started from 15Jan2021: Runny nose started about 8-10 hours after her injection. Stated that it was not bad, she would just have to blow her nose really good every so often. She said that she has not had to blow her nose today since she had been up. She said that the vaccine was sitting on the table and they just told her it was the Pfizer BioNTech vaccine. She did not have her vaccination card with her at the time of the call. The patient had recovered from weakness on 18Jan2021, recovered from increased heart rate and soreness at the injection site on 17Jan2021; she was recovering from more tired, runny nose, and she had not recovered from diarrhea. Reporter seriousness for increased heart rate, runny nose and soreness at the injection site was not serious. The reporter (nurse) considered the events more tired, weakness, diarrhea, runny nose and soreness at the injection site were related to bnt162b2, and relatedness of bnt162b2 to reaction increased heart rate was unknown. Information on the lot/ batch number has been requested.

Other Meds: ALBUTEROL [SALBUTAMOL]

Current Illness:

ID: 1000180
Sex: F
Age:
State:

Vax Date: 01/14/2021
Onset Date:
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: fever; body aches; This is a spontaneous report from a non-contactable consumer (patient). A female patient of unspecified age received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 14Jan2021 19:00 at single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. Patient previously received the first dose of BNT162B2 on 23Dec2020 and experienced arm sore. After the second dose, patient experienced fever and body aches. Outcome of the events was unknown. No follow-up attempts are possible, information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1000181
Sex: F
Age:
State: FL

Vax Date: 01/18/2021
Onset Date: 01/18/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Bad headache; This is a spontaneous report from a contactable consumer (patient). A 65-year-old female patient received BNT162B2 first dose on 18Jan2021 15:30 on left arm at single dose for COVID-19 immunization at Parking lot of a big stadium. Medical history included stressed and headache, both from 18Jan2021 before vaccine and medication to help sleep. Concomitant medication included ongoing clonazepam (KLONOPIN) tablet at 2mg pill at night to help sleep. Vaccine not Administered at Military Facility. No History of all previous immunizations with the Pfizer Vaccine considered as suspect. No Additional Vaccines Administered on Same Date. No Prior Vaccinations within 4 weeks. She is calling because she got the vaccine today and she has a bad headache. She mentioned she knows headache is a possible side effect. However, she is calling to see what she can take or what she cannot take for the headache. She stated before getting the vaccine she was stressed and had a headache that had started today, 18Jan2021, before she got the vaccine. She mentioned she was waiting 3.5 to 4 hours before getting the shot and that is when the headache started. However, after getting the vaccine it has gotten worse and it is to the point where she wants to place an icepack on her face. Stated it could be situational. She knows she was in the car for at least 5 hours. She also mentioned the paperwork we provide with a list of symptoms should also have listed what medications she can or cannot take. She finds it troubling that we do not have the listed on the paperwork. We have headache could be a possible symptom, but no information on what can be taken for symptoms. She also mentioned she needed her reading glasses to attempt to read the patient card provided that list the lot number and details regarding date for next dose. She then stated after looking at the card it is impossible to read. She cannot read the person's handwriting. The lot number is so messy. She believes it is: L2 7 or 8, 922 or 422, something like that, she cannot really tell the handwriting is so messy. The event not require a visit to Emergency Room or Physician's Office. The outcome of the event was not recovered. Information on the lot/batch number has been requested.

Other Meds: KLONOPIN

Current Illness:

ID: 1000182
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: fever that lasted for a day then it resolved; This is a spontaneous report from a Pfizer sponsored program IBCC (Inbound Call Center for HCPs). A non-contactable consumer reported for a male patient (her husband). A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced fever that lasted for a day then it resolved on an unspecified date with outcome of recovered on an unspecified date. Caller wanted to know any data available for covid vaccine use in GBS (Guillain-Barre syndrome) and autoimmune disorder. caller sated her husband had reaction to the vaccine, fever that lasted for a day then it resolved. caller stated she has autoimmune disease also so wanted to know does the vaccine worsen the symptoms. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1000183
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: dull headache; body aches; This is a spontaneous report from a contactable consumer, the patient received from Pfizer. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration on an unspecified date as a single dose for COVID-19 vaccination. Medical history and concomitant medication were not reported. On an unspecified date, the patient experienced dull headache and body aches. The clinical outcome of dull headache and body aches was unknown. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1000184
Sex: M
Age:
State: AZ

Vax Date: 01/17/2021
Onset Date: 01/19/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: dizziness; This is a spontaneous report from a contactable consumer (patient's wife). This consumer reported same events for two patients. This is the second of two reports. A male patient (husband) of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number EL1284 and expiry date unknown) via unspecified route of administration on 17Jan2021 at single dose for Covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient's wife reported that she got the shot on Sunday (17Jan2021) along with her husband (patient). The patient's wife informed that all of the sudden she was getting dizzy, otherwise they had no problem. She even made a second appointment. The reporter informed that her husband (patient) was getting it also. The reporter informed that the dizziness for both of them started today on 19Jan2021. The outcome of the event dizziness was unknown.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021061733 same reporter/drug/event and different patients

Other Meds:

Current Illness:

ID: 1000185
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 02/04/2021
Hospital: Y

Lab Data:

Allergies:

Symptoms: Had a stroke; This is a spontaneous report from a contactable consumer via Pfizer-sponsored programs. A male patient (reporter's husband) of an unspecified age received first single dose of BNT162B2 (Solution for injection, batch/lot number and exp date not reported), via an unspecified route of administration on an unspecified date for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient got the first dose of Covid vaccine on an unspecified date (Friday) at 12:35 PM, and had a stroke on Saturday morning at 10:30AM and was confined at the hospital (date/s unspecified) at the time of reporting. Reporter asked if there was any correlation or any fact sheets available with the vaccine and the stroke that happened to the patient. The outcome of the event was unknown. Information about lot number and expiry date for the suspect product will be requested in follow-up attempts.

Other Meds:

Current Illness:

ID: 1000186
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: patient bled, and a proportion of vaccine in the syringe was not administered; patient bled, and a proportion of vaccine in the syringe was not administered; This is a spontaneous report from a contactable pharmacist. A patient of unspecified age and gender received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot/batch number and expiration date not provided), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient previously took first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) at single dose for COVID-19 immunization. The pharmacist had a question regarding incomplete administration of 2nd dose of bnt162b2. While one patient was given a vaccine, patient bled, and a proportion of vaccine in the syringe was not administered on an unspecified date. The pharmacist asking was there any information about giving a third dose to those who received invalid second dose. The outcome of the events was unknown. Information on the lot/batch number has been requested.; Sender's Comments: Based on temporal association, the causal relationship between bnt162b2 and the event haemorrhage cannot be excluded. The information available in this report is limited and does not allow a medically meaningful assessment. This case will be reassessed once additional information becomes available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees, and Investigators, as appropriate.

Other Meds:

Current Illness:

ID: 1000187
Sex: F
Age:
State: OR

Vax Date: 01/15/2021
Onset Date: 01/16/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Body aches; Chills; Headache; Arm was really, really sore - the whole arm; This is a spontaneous report from a contactable consumer (patient who is a mental health therapist). A 50-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number and Expiration Date were not reported), via an unspecified route of administration in left arm, on 15Jan2021 at 16:00 (4 PM), at a single dose, for COVID-19 immunization. The patient had no medical history and concomitant medications. No other vaccines were given the same day or 4 weeks prior. No problem with vaccines in past that she can recall from childhood. The patient received the vaccine last Friday (15Jan2021) and side effects started early evening Saturday (16Jan2021) or late afternoon. The patient had body aches, a few chills, headache, and her arm was really, really sore - the whole arm. At the time of reporting, all are way better. The patient was recovering from the events. Information about lot number and expiration date for the suspect product will be requested in follow-up attempts.

Other Meds:

Current Illness:

ID: 1000188
Sex: F
Age:
State:

Vax Date: 01/15/2021
Onset Date:
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: very itchy throat; can't sleep; This is a spontaneous report from a contactable consumer (patient). A female patient of unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE) via an unspecified route of administration on 15Jan2021 as a single dose for COVID-19 immunization. Medical history included "underlying conditions." Concomitant medications were not reported. The patient reported after she received the vaccine her throat was very itchy and no pain on an unspecified date. It bothered her so much that she couldn't even sleep. She wanted to know if this was a normal side effect to be very itchy in the throat. She had called out of work since Monday (18Jan2021) and did not want to go to the emergency room where people had COVID. She did not want to be around people. The outcomes of the events were unknown. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow-up.

Other Meds:

Current Illness:

ID: 1000189
Sex: M
Age:
State: OH

Vax Date: 01/18/2021
Onset Date:
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: anxious; This is spontaneous report from a contactable consumer (patient's niece). A 92-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiry date were unknown) via an unspecified route of administration, on 18Jan2021, at a single dose, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Patient's niece reported that her uncle had the Pfizer vaccine yesterday and now was acting really anxious. She was wondering if this is normal. Outcome of the event was unknown. Information on lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1000190
Sex: F
Age:
State: OR

Vax Date: 01/14/2021
Onset Date: 01/17/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: left paraclavicular lymphadenopathy; This is a spontaneous report from a contactable nurse (patient) reported that a 30-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3246), intramuscular on the left arm on 14Jan2021 14:30 at a single dose for Covid-19 immunization. The patient's medical history and concomitant medications were not reported. Patient was not pregnant. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231), intramuscularly on the left arm on 23Dec2020 10:45 for Covid-19 immunization. It was reported that approximately 72 hours (17Jan2021) after second dose, the patient developed left paraclavicular lymphadenopathy. No treatment received was reported for the reported event. The outcome of the event was not recovered.

Other Meds:

Current Illness:

ID: 1000191
Sex: F
Age:
State: CA

Vax Date: 01/05/2021
Onset Date: 01/05/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210118; Test Name: antibodies; Result Unstructured Data: Test Result:does not have any

Allergies:

Symptoms: tested for antibodies, and does not have any; States her second dose was on 05Jan2021, that was day number 18 after the first one.; States her second dose was on 05Jan2021, that was day number 18 after the first one.; This is a spontaneous report from a Pfizer-sponsored program from a contactable pharmacist (patient). A 47-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, on 05Jan2021 at single dose (reported as 0.3, unit not provided) for COVID-19 immunisation, by injection to left arm. Medical history was none. Concomitant medications included levothyroxine sodium (SYNTHROID). Historical vaccine included first dose of BNT162B2 on an unknown date for COVID-19 immunisation. The patient states her second dose was on 05Jan2021, that was day number 18 after the first one. On 18Jan2021 the patient was tested for antibodies, and does not have any. She was expecting to have antibodies. She is not sick, she did not get sick, but because she didn't have antibodies it is upsetting, but there is nothing going on with body because she doesn't have the antibodies. Calling to find out what she should do now, if she needs to be revaccinated. The event was reported serous as medically significant. Outcome was not recovered. Method of assessment: Global Introspection was related, there is no reason why she wouldn't develop antibodies normally.; Sender's Comments: The 47-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), on an unknown date, and then received second dose on 05Jan2021, that was day number 18 after the first one. On 18Jan2021 the patient was tested for antibodies, and does not have any. There is possibility of false negative COVID-19 antibody test. The exact reason was unknown. The case will be reassessed should additional information become available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics committees and Investigators, as appropriate.

Other Meds: SYNTHROID

Current Illness:

ID: 1000192
Sex: F
Age:
State:

Vax Date: 09/01/2020
Onset Date:
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Name: MRI; Result Unstructured Data: Test Result:Unknown results

Allergies:

Symptoms: headache; This is a spontaneous report received from a non-contactable consumer (patient) via Medical Information Team. An 80-year-old female patient received pneumococcal 13-valent conjugated vaccine (diphtheria crm197 protein) (PREVNAR 13; Solution for injection in pre-filled syringe), via an unspecified route of administration on Sep2020 at single dose for immunization. The patient medical history and concomitant medications were not reported. It was reported that, the patient received a dose of pneumococcal 13-valent conjugated vaccine (diphtheria crm197 protein) on Sep2020 after her physician recommended her to be immunized with the vaccine after the risk of Pneumonia and COVID-19 concomitantly. The patient developed a headache on an unspecified date after the administration of the vaccine pneumococcal 13-valent conjugated vaccine (diphtheria crm197 protein) and that persists up to this day. The patient reports that her Physician had studied her medical conditions with tests, and MRI and different medications but it has not taken away the headaches. The outcome of the event was reported as unknown. No follow-up attempts are possible. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1000193
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Diverticulitis; little bit of pain; This is a spontaneous report from a Pfizer sponsored program. A contactable consumer (patient) reported that a female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiry date: unknown), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient got her first shot of covid vaccine, sometimes she have Diverticulitis a little bit of pain and she wanted to find out if it's ok to take antibiotics and also get the second shot on the 28th. The outcome of the events was unknown. Information on the Lot/Batch number has been requested

Other Meds:

Current Illness:

ID: 1000194
Sex: M
Age:
State: CA

Vax Date: 01/10/2021
Onset Date: 01/10/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Stomach upset; This is a spontaneous report from a contactable pharmacist. A 47-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: EL3246), intramuscular in the left arm on 10Jan2021 (at the age of 47-year-old) as a single dose for COVID-19 immunization. Medical history included hypertension. The patient did not have any allergies to medications, food, or other products. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient's concomitant medications were not reported. . The patient did not receive any other vaccines within four weeks prior to the vaccination. Historical vaccine included Dose 1 of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: EL0140), intramuscular, left arm on 20Dec2020 for COVID-19 immunization. On 10Jan2021, the patient experienced stomach upset. The patient took Compazine for the stomach upset. The clinical outcome of the event stomach upset was recovered. It was also reported that since the vaccination, the patient had not been tested for COVID-19.

Other Meds:

Current Illness:

ID: 1000195
Sex: F
Age:
State: FL

Vax Date:
Onset Date:
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: shoulder was sore and painful; This is a spontaneous report from a contactable consumer (patient's husband). A female patient of an unspecified age received the first dose of bnt162b2 (BNT162B2), Batch/lot number was not provided, via an unspecified route of administration from an unspecified date as a SINGLE DOSE for COVID-19 vaccination. Medical history was none. There were no concomitant medications. The consumer reported his wife had the same vaccine and her shoulder was sore and painful on an unspecified date. They still have pain when they move their shoulder. The consumer later clarified that her shoulder is not sore anymore. They put an ice on their shoulder. Outcome of the shoulder was sore and painful was recovered on unknown date. Information on lot number/batch number was requested.

Other Meds:

Current Illness:

ID: 1000196
Sex: F
Age:
State: NJ

Vax Date: 01/13/2021
Onset Date: 01/01/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Name: temperature; Result Unstructured Data: Test Result:99; Test Date: 20210115; Test Name: temperature; Result Unstructured Data: Test Result:lower

Allergies:

Symptoms: Aches and pains; Fatigue; Fever/My temperature was 99 which "generally" (not clarified) my temperature is usually 97; Arm was extremely painful; Joint pain; Headache; Could not work today because I was not feeling good; This is a spontaneous report from a contactable consumer (patient). A 63-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE Lot), via an unspecified route of administration, on 13Jan2021 (at the age of 63-years-old) as a single dose for COVID-19 vaccination. Medical history includes heart disorder. Concomitant medication included: Simvastatin, Atenolol, and medicine for my "heart". The patient reported that she received the first dose on 23Dec2021 and stated she had no reaction. On an unspecified date, the patient stated "I could not work today because I was not feeling good from the vaccine. I got it on the 13th I had off some work yesterday so I had a temperature aches and pains, fatigue and I had to call out last night. Today I am running still very slight fever, aches and pains - so it is improving." The first day, I was fine. I got it at the end of the day. The second day my arm was not red or anything but it was extremely painful, joint pain, headache, fatigue and my temperature was 99 (my temperature is usually 97). Today the temperature is lower and that does not hurt as much." The clinical outcome of the events malaise, aches and pain, fatigue, pyrexia, pain in arm, joint pain, and headache was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds: SIMVASTATIN; ATENOLOL

Current Illness:

ID: 1000197
Sex: F
Age:
State: AZ

Vax Date: 01/05/2021
Onset Date: 01/01/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Name: height; Result Unstructured Data: Test Result:5' 7"; Test Name: weight; Result Unstructured Data: Test Result:175 lbs

Allergies:

Symptoms: Do not believe he gave it IM, I believe he gave it subQ; Redness; Swelling; heat coming out; Skin lesions 4.5 to 7cms/Red spot on my arm; Low grade temperature elevation; Fatigue; This is a spontaneous report from a contactable physician (patient). A 67-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number: EH9899, reported as "SARS-COV-2 then it says Pfizer EH9899", expiry date: Unknown), subcutaneous on 05Jan2021 at single dose for COVID-19 immunization (reported as "To not get COVID 19"). Medical history included hypothyroidism. Concomitant medication included levothyroxine sodium (SYNTHROID) 25mcg, once a day for hypothyroidism. The patient got the vaccine last Tuesday (05Jan2021). When she got the vaccine, the gentleman was from military who gave the vaccine. The patient does not believe that he gave it intramuscular (IM), she believed that he gave it "subQ" because she had no muscle tenderness and "skin a 4.5 by 7cm skin reaction", and it was nowhere near the deltoid muscle. The patient had a high degree of suspicion that he gave it "subQ" (subcutaneous). When asked for the anatomical location of administration, the patient stated that "He gave it on my right arm but it was not into the deltoid, I think he gave it subcutaneously. I am not positive of that but missed the deltoid, it was lower, it was below the deltoid, it was in between the deltoid and the bicep and I am assuming it was subQ because none of my muscles were sore at all after getting the vaccine, accept that big red spot on my arm". Patient asked "Now my question to you is because I looked through all your literature and I can't find anything about this". Since then the skin lesion within a couple of days it was up to about 4.5 to 7cms. It was still about that size however the redness has gone way down, "the not redness", just pink, the swelling was almost gone. The heat coming out of it was almost gone. The patient mentioned that the actual skin region was much better, it was still about the same size though. Patient was not too worried about that and stated "what am concerned about is what I've also have is a low grade temperature elevation and some fatigue. If I got it on 3 O'clock on Tuesday the 5th that would be day 9. Is the 9 days post injection for dose 1 to still have a low grade temperature elevation and some fatigue. Is that acceptable or does that indicate a problem?". Patient stated the she went to her internist and he had a look at it and he said "I had no idea, he said that they just don't have experience like this. Do you have a phone number that I can talk to somebody?". The patient was about 5' 7" (height) and about 175 pounds (weight) approximately. The patient stated that fatigue and temperature elevation started one or two days after the vaccine (Jan2021). Patient reported that she still have it. The fatigue was much less but it was there and low grade temperature elevation was still there. There was no investigation assessment. The patient assessed that the events swelling, redness, skin lesions, temperature and fatigue were related to COVID-19 vaccine, also reported as "Yes, because I never had that before and I am not taking anything now. So, it is like yes. It is definitely because that. The two main symptoms I am asking about are the fatigue and the low grade temperature elevation". Outcome of the events fatigue and skin lesion, redness, swelling and heat coming out was recovering, for low grade temperature elevation was not recovered.

Other Meds: SYNTHROID

Current Illness:

ID: 1000198
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Name: COVID; Test Result: Positive

Allergies:

Symptoms: Tested positive for COVID in between the doses for the vaccines; Tested positive for COVID in between the doses for the vaccines; This is a spontaneous report from a Pfizer sponsored program. A contactable registered nurse (not the patient) reported a patient of unspecified age and gender received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; COVID Vaccine a Pfizer product; lot number: EK9231) via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. Reporter added they were exposed before getting it and did not realize that they were exposed. The patient was tested positive for COVID in between the doses for the vaccines, on an unspecified date. She was wondering what we suggest they do with the second dose. The outcome of event was unknown.; Sender's Comments: Based on the information currently available, a lack of efficacy with BNT162B2 in this patient cannot be completely excluded.

Other Meds:

Current Illness:

ID: 1000199
Sex: M
Age:
State: NY

Vax Date: 12/30/2020
Onset Date: 01/12/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210112; Test Name: PCR Test/ COVID-19; Test Result: Positive ; Test Date: 20210114; Test Name: rapid test; Test Result: Negative

Allergies:

Symptoms: positive COVID-19 test with no symptoms; positive COVID-19 test with no symptoms; This is a spontaneous report from a Pfizer-sponsored program from a contactable physician (patient). A 56-year-old male patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot EL1284), via an unspecified route of administration on 30Dec2020 at single dose for COVID-19 immunisation. Medical history and concomitant medications were none. The patient had a PCR test on 12Jan2021 and was COVID-19 positive, asymptomatic. The patient had a rapid test on 14Jan2021 and came out negative. The doctor was asking if he can be able to get the second vaccine a longer than 3 weeks which is in the 6th week, asking if it could make a difference since he was tested positive. The outcome of the events was recovered on 14Jan2021.; Sender's Comments: The patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE) on 30Dec2020, and a PCR COVID-19 test positive on 12Jan2021, asymptomatic. No complete effect of the suspect vaccine could be reasonably achieved from first dose to protect from the targeted infection. Further information is needed for a full meaningful medical assessment.

Other Meds:

Current Illness:

ID: 1000200
Sex: U
Age:
State: PA

Vax Date:
Onset Date:
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Allergic reaction; This is a spontaneous report from a contactable Other HCP. A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced allergic reaction on an unspecified date. Event outcome was unknown. Information on Lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1000201
Sex: F
Age:
State: MO

Vax Date: 01/15/2021
Onset Date: 01/15/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: I feel like I have a lump in my throat and I have a hard time when I lay down breathing it feels like just something caught in my throat and it was not there before; I feel like I have a lump in my throat and I have a hard time when I lay down breathing it feels like just something caught in my throat and it was not there before; This is a spontaneous report received from a contactable consumer (who is also the patient). A 77-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK4176, expiry date: unknown), via an unspecified route of administration, on 15Jan2021, at single dose, for COVID-19 immunization. Medical history included inflammatory bowel disease. Concomitant medication included diphenoxylate from 14Jan2021 for inflammatory bowel disease. The patient stated, "I feel like I have a lump in my throat and I have a hard time when I lay down breathing it feels like just something caught in my throat and it was not there before. I never had that before and it feels like I have a hard time when I lay down to breathe and I was wondering if that has anything to do with the side effect of this vaccine." When asked for treatment, patient stated, "No, because it just started yesterday (15Jan2021). That is why I called you. I wanted to know if that dangerous. Do I have to go to an emergency clinic because today is Saturday and everything is closed or should I just do not worry about it." The outcome of the events was unknown.

Other Meds: DIPHENOXYLATE

Current Illness:

ID: 1000202
Sex: U
Age:
State:

Vax Date: 01/14/2021
Onset Date: 01/01/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: woke up with little aches; Dizzy; Little breathless; Heart goes pumping; Nervous; Very tired; I don't know if I'm dehydrated; Not feeling well; This is a spontaneous report from a contactable consumer (patient). A 77-year-old patient of unspecified gender received bnt162b2 (BNT162B2, lot number and expiry date were not reported), via an unspecified route of administration, on 14Jan2021 at a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient received the COVID vaccine on Thursday, 14Jan2021. The patient was doing well on the day of vaccination. The following day, 15Jan2021, the patient was very tired. At the morning of the report, 16Jan2021, the patient woke up with little aches, tired, but they don't know what it was. The night before, 15Jan2021, the patient got a little get upset from something, a door man, or some noise. But all of a sudden, they got a little breathless, and I felt little dizzy. And the patient had some orange juice, (Beverage company name withheld) and a little cereal. The patient commented, "I guess, it's the dizziness, lightheaded and you know, your heart goes pumping a little, a little dizzy and things like that. So, I just thought I'd call." The patient added, "I have Allegra here, I didn't take it though. I have a little (Beverage company name withheld). I just got a little nervous, I live alone and except the (Beverage company name withheld). I hope, I don't know if I could go or act to sleep or just a little lightheaded, you know, breathless and dizzy and I wasn't sure of that. And it's two days, Thursday afternoon and it's Friday. I don't know, this is strange, I don't know if I'm dehydrated or this reaction to the vaccine, Pfizer. I can't tell you, I am just a little scared. I am not feeling well, and I wanted to know if there is anything dangerous? Or anything I can do?" The patient's second dose was scheduled on 04Feb2021. Outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1000203
Sex: M
Age:
State: FL

Vax Date: 01/12/2021
Onset Date: 01/13/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Name: blood sugar; Result Unstructured Data: Test Result:come down again; Test Name: blood sugar; Result Unstructured Data: Test Result:high; Test Date: 20210113; Test Name: blood sugar; Result Unstructured Data: Test Result:elevated; Comments: elevated a whole lot/ it went real high

Allergies:

Symptoms: sugar was elevated a whole lot/went real high; This is a spontaneous report from a contactable consumer (patient). A 79-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: unknown), via an unspecified route of administration on 12Jan2021 at single dose for Covid-19 immunization (wanted to get because of the virus). The patient's medical history included hard of hearing and diabetes (reported as "diabetes and stuff). Concomitant medications included empagliflozin (JARDIANCE), dulaglutide (TRULICITY), and other medications (as reported " I take stuff for blood pressure all kind of stuff"). The patient reported that he got the vaccine on Tuesday (12Jan2021), he stated that he has diabetes and stuff and he noticed on Wednesday, Thursday, Friday his sugar was elevated a whole lot and he thought that would be possibly from the vaccine or it might be stressed because the Covid (unspecified). He stated that he doesn't know but it's unusual, he means it went real high. He wanted to know if there are any reports of like affects it might cause on hi sugar to go high. The patient checked this morning (unspecified date) it was high and just checked about 20 minutes ago and it has come down again so (further not clarified)." The patient mentioned that he takes Jardiance and Trulicity, once a week; he took Trulicity this morning (unspecified date) and stated, "so that probably helped". He had an unspecified laboratory test about 3 months ago, and there was no problem." The outcome of event was unknown. Information on the lot/batch number has been requested.

Other Meds: JARDIANCE; TRULICITY

Current Illness:

ID: 1000204
Sex: F
Age:
State: NY

Vax Date: 01/12/2021
Onset Date: 01/12/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Did get a reaction and my hands swelled up about 20 minutes after the vaccine and my tongue swelled up; Doctor said I cannot take the 2nd dose of the vaccine; Did get a reaction and my hands swelled up about 20 minutes after the vaccine and my tongue swelled up; Doctor said I cannot take the 2nd dose of the vaccine; This is a spontaneous report from a contactable consumer (patient). A 69-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EH9899 and expiration date Mar2021), via an unspecified route of administration first dose on 12Jan2021 at single dose for covid-19 immunisation. The patient's medical history included Asthma, Allergy, and Penicillin allergy. Concomitant medication included fexofenadine hydrochloride (ALLEGRA) for allergy at 180 mg, daily, budesonide (PULMICORT) for Asthma at Pulmicort is a inhaler 180, 2 puffs a day, montelukast sodium (SINGULAIR) for Asthma at 10 mg. Historical vaccine includes Tetanus and experienced allergic reaction. Past drug includes Sulphur and experienced allergy. It was reported that the patient had the vaccine on 12Jan2021 and patient was working in long term care "administrator". The patient did get a reaction and the patient hands swelled up about 20 minutes after the vaccine and her tongue swelled up. The patient did take Benadryl. The patient called her primary care doctor and was told to stay on the Benadryl and the patient was okay. The patient stated that the pharmacist that gave her the vaccine gave the Benadryl right away when the patient started swelling up. The patient spoke to her allergist and stated that she cannot take the second dose vaccine. So, the patient was concerned about her coverage because she work in a long term case. The doctor would not give me the shingle vaccine (unspecified vaccine) because they were afraid the patient would have a reaction to that. The outcome of the events was unknown.

Other Meds: ALLEGRA; PULMICORT; SINGULAIR

Current Illness:

ID: 1000205
Sex: F
Age:
State: TX

Vax Date: 01/14/2021
Onset Date: 01/01/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: acting weird and wouldnt eat; UTI; Aspirations phenomena; This is a spontaneous report from a Pfizer Sponsored Program Pfizer First Connect. A female patient of an unspecified age started to receive bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 14Jan2021 at single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The reporter was calling about mother. Said Mom is in E.R. Had received covid vaccine on Thursday. Friday she was ok. Saturday mom was acting weird and wouldn't eat. Saturday night she was thrashing around and wouldn't settle down so they took mom to E.R. was diagnosed with Aspirations phenomena and UTI. Treated the UTI then put her in nursing home. The outcome of the events was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm